546-67-8

Basic information

• Product Name: Lead tetraacetate
• Synonyms: Lead(IV) acetate, 96% dry weight, stabilized;Lead(Ⅳ) Acetate 〔Lead(Ⅳ) Tetraacetate〕;Monolead(II);tetraacetate;LTA;LEAD ACETATE;LEAD(+4)ACETATE;LEAD(IV) ACETATE
• CAS NO: 546-67-8
• Molecular Formula: 4C₂H₃O₂*Pb
• Molecular Weight: 443.38
• EINECS: 208-908-0
• Product Categories: Organic-metal salt;Classes of Metal Compounds;Oxidation;Pb (Lead) Compounds;Synthetic Organic Chemistry;Typical Metal Compounds;metal acetate salt
• Mol File: 546-67-8.mol
• Article Data: 1

Chemical Properties

• Melting Point: 175-180 °C
• Boiling Point: 118.1°C
• Flash Point: 40°C
• Appearance: White to light orange-pink/Crystalline Powder
• Density: 2,28 g/cm3
• Vapor Pressure: 13.9mmHg at 25°C
• Storage Temp.: 0-6°C
• Water Solubility: Decomposition
• Sensitive: Moisture Sensitive
• Stability: Stable. Moisture sensitive. Incompatible with water, most metals.
• Merck: 14,5423
• BRN: 3595640
• CAS DataBase Reference: Lead tetraacetate(CAS DataBase Reference)
• NIST Chemistry Reference: Lead tetraacetate(546-67-8)
• EPA Substance Registry System: Lead tetraacetate(546-67-8)

Safety Data

• Hazard Codes: T,N,O
• Statements: 61-8-20/22-33-35-50/53-62
• Safety Statements: 53-45-60-61-36/37/39-26-17
• RIDADR: UN 2923 8/PG 2
• WGK Germany: 3
• RTECS: AI5300000
• F: 10-21
• TSCA: Yes
• HazardClass: 6.1
• PackingGroup: III
• Hazardous Substances Data: 546-67-8(Hazardous Substances Data)

Usage

Chemical Description

Lead tetraacetate is a chemical reagent used in organic chemistry to oxidize alcohols to aldehydes or ketones.

InChI:InChI=1/4C2H4O2.Pb/c4*1-2(3)4;/h4*1H3,(H,3,4);/q;;;;+2/p-4

Upstream product

• 108-24-7 acetic anhydride 
• 64-19-7 acetic acid 
• 301-04-2 lead acetate 
• 75-15-0 carbon disulfide 
• 938-81-8 N-nitrosoacetanilide 
• 628-51-3 diacetoxymethane 
• 127-09-3 sodium acetate 
• 6080-56-4 lead(II) acetate trihydrate 

Downstream Products

• 111-30-8 Glutaraldehyde 
• 96-48-0 4-butanolide 
• 109-06-8 α-picoline 
• 108-89-4 picoline 
• 35262-78-3 3-benzoyl-3,4,5-triphenyl-3H-furan-2-one 
• 42866-92-2 2-(4-methoxyphenyl)acetaldehyde dimethyl acetal 
• 105476-15-1 1-acetoxy-1-methoxy-2-(4-methoxy-phenyl)-ethane 
• 632-92-8 2,4-dimethyl-1,3,5-trinitrobenzene 
• 36639-40-4 2,4,6-cycloheptatriene-1-carboxaldehyde dimethyl acetal 
• 79-20-9 acetic acid methyl ester 
• 15356-27-1 4,5-cyclohexylidenedioxy-3-hydroxytetrahydrofuran-2-carbaldehyde 
• 57-13-6 urea 
• 768-19-4 2-Methyl-s-triazolo<1,5-a>pyridin 
• 19791-95-8 α-hydroxyhippuric acid 

Relevant articles and documents

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Metal hydrates and salts of carboxylic acids

A metal salt of a carboxylic acid is formed by contacting a carboxylic acid with an activated metal. The activated metal is formed by combining a first metal with a second metal which has an affinity for hydrogen in the presence of a proton source. Typically, an activated aluminum is formed from a highly pure aluminum rod combined with an alloy of indium and gallium in the presence of hydrochloric acid. The addition of excess water in the presence of the carboxylic acid and activated metals forms a polymeric metal salt from a water soluble carboxylic acid.